The Use of Probiotic Megasphaera elsdenii as a Pre-Harvest Intervention to Reduce Salmonella in Finishing Beef Cattle: An In Vitro Model

Abstract

Reducing Salmonella in cattle may mitigate the risk of transmission through the food chain. Megasphaera elsdenii (ME) is a microorganism found naturally in the bovine rumen that can be administered as a probiotic to mitigate ruminal acidosis. Understanding the impact of feeding ME to Salmonella populations in cattle was the objective of this study. Bovine ruminal fluid (RF) and feces were inoculated with antibiotic susceptible or resistant Salmonella and treated with varying concentrations of ME. Salmonella was enumerated at 0, 24, 48, and 72 h using the most probable number (MPN). Volatile fatty acids (VFAs) and pH were recorded from non-inoculated samples. Treating RF with ME did not significantly impact Salmonella concentration or VFA production (p > 0.05). The pH of RF and feces decreased over time (p ≤ 0.05). Salmonella concentration declined in feces, with the largest reduction of 1.92 log MPN/g and 1.05 log MPN/g observed for antibiotic susceptible Salmonella between 0 and 72 h by the 2.5 × 10⁵ CFU/g and control (0.0 CFU/g) concentration of ME, respectively. Treating RF with ME did not impact Salmonella concentration. Salmonella concentration in feces decreased, although ME must be further investigated before a conclusion regarding efficacy in vitro can be determined.

1. Introduction

Throughout production, cattle are exposed to a variety of microorganisms in the feedlot environment. Antibiotics historically have been administered sub-therapeutically as growth promotants to optimize performance and increase profits. In January of 2017, the Food and Drug Administration’s ban on the use of “medically important” antibiotics for growth promotion became effective [1,2]. This, coupled with public health implications associated with a rise in antibiotic resistance [1] among pathogenic microorganisms, emphasizes the need for novel management practices to control microbial populations without introducing selective pressure associated with “medically important” antibiotics.

Understanding the impact of alternative animal husbandry practices to control foodborne pathogens, such as Salmonella, in cattle should also be prioritized. As Acuff and Dickson summarize in their recent book [3], the relationship between these pathogens and cattle is well-documented. This is further complicated by the fact that cattle often show no clinical symptoms of infection while shedding Salmonella in their feces [4,5,6] and/or harboring Salmonella in their lymph nodes [7]. In a 2014 review paper, Wells et al. [8] reviewed the body of research seeking to understand relationships between pathogens and other factors, such as diet and microbiome. Although these and other factors represent complex relationships within the host, it is clear that diet can impact cattle’s pathogen shedding status.

Supplementing cattle with a direct-fed microbial (DFM) has been investigated as a pre-harvest intervention to control foodborne pathogens while also improving production efficiency [9,10,11]. Megasphaera elsdenii is a lactic acid-utilizing bacterium that plays an important role in the rumen microbiome [12,13]. This microorganism utilizes lactate and mitigates ruminal acidosis (RA), which can occur as a result of feeding cattle diets containing relatively large proportions of cereal grains and other concentrates. Lactate utilization by M. elsdenii results in the production of VFAs (butyrate and acetate from d-lactate) [14] and moderation of ruminal pH [13]. Although M. elsdenii has demonstrated value as a mitigant for RA, published literature is lacking regarding the impact of this probiotic on Salmonella shedding in cattle. Previous publications suggest that an increase in fecal VFAs results in decreased E. coli O157:H7 populations in the hindgut of cattle [15,16]. Recognizing that M. elsdenii produces VFAs from lactate in the rumen, it could be hypothesized that M. elsdenii may also be present and producing VFAs in the hindgut, thereby reducing Salmonella carriage in the rumen and entire gastrointestinal tract, resulting in a reduction in fecal shedding.

The objective of this study is to use an in vitro challenge model previously developed by our team [17] to determine the efficacy of M. elsdenii at reducing antibiotic susceptible and resistant Salmonella populations in cattle feces and ruminal fluid. The data generated may provide preliminary information to support a larger in vivo cattle feeding trial.

2. Materials and Methods

2.1. Experimental Design

An in vitro challenge model described by Page et al. [17] was utilized to determine if M. elsdenii is effective at reducing Salmonella populations in the rumen and feces of cattle. This study was completed as a completely randomized design. Antibiotic susceptible and resistant Salmonella serotypes were inoculated into ruminal fluid and feces, with or without M. elsdenii, and quantified throughout a 72 h period. All procedures were replicated three times and efficacy was determined based upon Salmonella reductions achieved by M. esldenii treated samples in comparison to the inoculated, untreated control. The pH and concentration of volatile fatty acids were also measured throughout the study from non-inoculated samples.

2.2. Culture Preparation

A two-strain Salmonella cocktail was prepared from one Salmonella Newport strain and one Salmonella Anatum strain, both of which were pansusceptible to the following veterinary antibiotics: amoxicillin/clavulanic acid, ampicillin, cefoxitin, ceftiofur, ceftriaxone, chloramphenicol, ciprofloxacin, gentamicin, nalidixic acid, streptomycin, sulfisoxazole, tetracycline, and trimethoprim/sulfamethoxazole. A second two-strain cocktail was prepared from one Salmonella Newport and one Salmonella Montevideo, both of which were resistant to one or more of the veterinary antibiotics listed above. Frozen stock cultures of each strain were streaked for isolation onto Xylose Lysine Desoxycholate (XLD) agar and incubated for 18–24 h at 37 °C. Following incubation, one isolated colony was selected from each plate, transferred to a 9 mL tryptic soy broth (TSB) tube, and incubated for 18–24 h at 37 °C. Following incubation, 1 mL of each strain was diluted in 0.1% peptone water (PW) to prepare separate antibiotic susceptible and resistant cocktails, each with an approximate concentration of 1.0 × 10⁶ CFU/mL.

2.3. Sample Preparation

Ruminal fluid and feces were collected from cattle at the Kansas State University Beef Cattle Research Center according to Institutional Animal Care and Use Committee approvals. Feces were collected from multiple animals and composited into one large fecal sample. The same procedure was followed for ruminal fluid. From the fecal and ruminal fluid composite samples, a 500 g portion was weighed for inoculation (target concentration of 1.0 × 10³ CFU/g to 1.0 × 10⁴ CFU/g). Briefly, 1 mL of cocktail was homogenized by shaking the ruminal fluid or hand massaging feces for 2 min. The inoculated 500 g was divided into 90 g portions (n = 5 for ruminal fluid and feces) into individual Whirl-Pak^® (Nasco, Madison, WI, USA) sample bags and M. elsdenii was added using Lactipro NXT^® (MS Biotec, Wamego, KS, USA), a commercially available freeze-dried M. elsdenii product that is commonly administered to feedlot cattle as an oral drench and has a guaranteed concentration of 5.0 × 10⁸ CFU/mL when rehydrated in the provided anaerobic diluent. Lactipro NXT^® was rehydrated using the anaerobic diluent provided with the Lactipro NXT^® product, based upon the 5.0 × 10⁸ CFU/mL guaranteed concentration, to achieve target concentrations of M. elsdenii in each sample. Briefly, from each prepared concentration, 10 mL were added to 90 g of ruminal fluid and feces (90 g of ruminal fluid or feces + 10 mL of M. elsdenii = 100 g of sample total) to prepare samples containing M. elsdenii at concentrations described in

Table 1. Addition of Lactipro NXT^® in 10 mL anaerobic diluent to achieve target concentrations of Megasphaera eldenii in cattle ruminal fluid and feces as an in vitro model.

Target Concentrations of M. elsdenii (CFU/g)
Control: 10 mL anaerobic diluent without M. elsdenii = 0
1.0 × 105
2.5 × 105
5.0 × 105
5.0 × 108

.

Thieszen et al. [18] investigated ruminal pH and VFA production in cattle orally drenched with 0, 25, 50, 75, and 100 mL of Lactipro NXT^® (previously known as Lactipro) per animal. The concentrations in Table 1 were selected to reflect similar concentrations to Thieszen et al. [18], with the addition of a 5.0 × 10⁸ CFU/g concentration that would simulate the growth of M. elsdenii in the rumen following Lactipro NXT^® administration. Recognizing that the rumen typically holds a minimum of 95 L (~25 gallons) [19], a ruminal volume of 100 L was used to calculate target concentrations for M. elsdenii to maintain the same concentration in each 100 g sample of ruminal fluid and feces (Table 1). These procedures were completed for each cocktail.

A set of ruminal fluid and fecal samples not inoculated with Salmonella (hereafter to referred to as non-inoculated) was also prepared according to Table 1 for Salmonella MPN (as previously described), as well as VFA and pH analyses as described in the Volatile Fatty Acid and pH Analyses section below. Therefore, the result of this sample preparation was three separate experiments for ruminal fluid and feces as follows: non-inoculated feces, non-inoculated ruminal fluid, feces inoculated with antibiotic-susceptible Salmonella, ruminal fluid inoculated with antibiotic-susceptible Salmonella, feces inoculated with antibiotic-resistant Salmonella, ruminal fluid inoculated with antibiotic-resistant Salmonella.

Following preparation of samples, individual sample bags were placed in anaerobic containers with an AnaeroGen (Oxoid, Lenexa, KS, USA) gas sachet and anaerobic indicator strip to simulate anaerobiosis of the bovine gastrointestinal tract. Anaerobic containers were stored on a shaking incubator set to 50 rpm and 38.6 °C to mimic peristaltic motion within the gastrointestinal tract and the body temperature of a bovine, respectively. Samples were removed from the shaking incubator and analyzed for Salmonella at 0, 24, 48, and 72 h using a repeated measures approach. Following sampling, the samples were returned to the anaerobic containers and incubator as described above.

2.4. Microbiological Analyses

Ruminal fluid and feces were enumerated via the most probable number (MPN) as described by Page et al. [17]. Briefly, at each time point, 10 g of each sample were homogenized in 90 mL of PW, serially diluted in 9 mL PW tubes, and used to inoculate a 3 × 7 matrix of Rappaport Vasiliadis (RV) broth. The RV MPN tubes were incubated for 18–24 h at 37 °C and then streaked onto Xylose Lysine Desoxycholate (XLD). The XLD plates were incubated for 18–24 h at 37 °C and examined for typical (black colonies) Salmonella growth. Salmonella growth on the XLD plate corresponded to a positive MPN tube. The presence or absence of Salmonella was recorded for each tube and the pattern of tubes was recorded for the 3 × 7 MPN matrix. The MPN CFU/g was calculated for each sample using the Environmental Protection Agency (EPA) MPN calculator [20]. Any RV tubes associated with questionable Salmonella growth on XLD were subjected to immunomagnetic separation (IMS) as described by Page et al. [17]. Briefly, anti-Salmonella Dynabeads (Applied Biosystems, Grand Island, NY, USA) were used with a KingFisher ML (Thermo Scientific, Waltham, MA, USA) according to manufacturer’s guidelines, and 50 µL of the resultant bead suspension were spread-plated onto XLD. The XLD plates were incubated and observed for characteristic Salmonella growth as previously described. Growth was associated with a positive RV tube and the MPN pattern was then finalized based upon these IMS data. Salmonella on XLD plates from non-inoculated and inoculated samples were agglutinated at random using Wellcolex^TM latex agglutination kits (Remel, Lenexa, KS, USA) to ensure that growth was being accurately reported.

2.5. Volatile Fatty Acid and pH Analyses

At each sampling point, the pH of each ruminal fluid and fecal sample was recorded using a calibrated benchtop pH meter with glass probe. Fecal samples were prepared for pH measurement by homogenizing 5 g with 20 mL of sterile water [21]. Following pH measurement, the homogenized fecal samples were centrifuged and supernatant collected for VFA analyses [21]. Concentrations of VFA were evaluated for each ruminal fluid and fecal sample at every time period. Briefly, concentrations of volatile fatty acids in ruminal fluid and feces were determined by gas chromatography using an Agilent 7890 gas chromatograph equipped with a flame ionization detector and bonded polyethylene glycol capillary column (DB-Wax Ul; 20 m length × 0.18 mm diameter × 18 µm film thickness; Agilent; Santa Clara, CA, USA). Hydrogen was used as the carrier gas and oven temperature was ramped from 50 to 240 °C at a rate of 30 °C/min.

2.6. Statistical Analyses

Three replications of the study were completed each for ruminal fluid and feces. Log MPN/g of Salmonella were analyzed as a repeated measures study using linear mixed models (MIXED procedure of Statistical Analysis Software; SAS 9.4, Cary, NC, USA) to determine impact of M. elsdenii on concentrations of Salmonella in cattle ruminal fluid and feces. Statistical analyses were performed separately for ruminal fluid and feces, as well as for non-inoculated, antibiotic-susceptible Salmonella, and antibiotic-resistant Salmonella samples (e.g., antibiotic-susceptible Salmonella inoculated in ruminal fluid was a single statistical model). Each sample bag served as the experimental unit. The best covariance structure was determined for each sample and inoculation type (e.g., ruminal fluid, non-inoculated), and then used in the model. Main effects of treatment, time, and the time × treatment interaction were evaluated at the 0.05 significance level. Means and standard error of the mean (SEM) were calculated for significant main effects and interactions using the LSMEANS statement with Tukey–Kramer to evaluate differences between means. Mixed-effects analyses with the Tukey–Kramer adjustment in GraphPad Prism 9.0 (San Diego, CA, USA) were used to analyze impact of M. elsdenii on VFAs and pH of non-inoculated samples. Main effects of treatment, time, and time × treatment interaction were evaluated at the 0.05 significance level.

3. Results

3.1. Microbiological Analyses

When feces were treated with varying concentrations of Megasphaera elsdenii and sampled at 0, 24, 48, and 72 h, the impact of treatment, time, and the treatment × time interaction was significant (p < 0.0001) for naturally occurring Salmonella in non-inoculated feces. Because the treatment × time interaction was significant, non-inoculated Salmonella data from feces are displayed and discussed according to sampling point (time) and Megasphaera elsdenii concentration (treatment). In general, the naturally occurring Salmonella concentration declined over time (

Table 2. Mean concentration (log₁₀ MPN/g) of naturally occurring Salmonella in non-inoculated cattle feces at 0, 24, 48, and 72 h following treatment with varying concentrations of Megasphaera elsdenii as an in vitro model.

Time Point (Hours)	Megasphaera elsdenii Target Concentration (CFU/g)
	0.0		1.0 × 105		2.5 × 105		5.0 × 105		5.0 × 108
	Salmonella Log MPN/g	SEM	Salmonella Log MPN/g	SEM	Salmonella Log MPN/g	SEM	Salmonella Log MPN/g	SEM	Salmonella Log MPN/g	SEM
0	1.52 A,a	0.01479	1.31 A,b	0.01479	1.46 A,a,c	0.01479	1.44 A,c	0.01479	1.63 A,d	0.01479
24	1.54 A,a	0.01688	1.18 B,b	0.01688	1.37 B,c	0.01688	1.05 B,d	0.01688	1.44 B,c	0.01688
48	1.37 A,a	0.09226	1.37 A,B,a	0.09226	1.43 A,B,a	0.09226	1.22 A,B,a	0.09226	1.40 A,B,a	0.09226
72	0.76 B,a	0.0765	0.65 C,a	0.0765	0.87 C,a	0.0765	0.67 C,a	0.0765	0.63 C,a	0.0765

Uppercase superscripts that vary within a column are statistically different (p ≤ 0.05) and are comparing one treatment across each sampling point. Lowercase superscripts that vary within a row are statistically different (p ≤ 0.05) and are comparing each treatment across a single sampling point. SEM indicates standard error of the mean.

) in non-inoculated feces. The largest reduction observed was 1 log MPN/g (p < 0.0001) between the 0 and 72 h time points in feces treated with 5.0 × 10⁸ CFU/g of M. elsdenii. However, naturally occurring Salmonella also declined (p < 0.0001) by 0.76 log MPN/g in the control feces (0.0 CFU/g of M. elsdenii) not inoculated with Salmonella. At the 72 h timepoint, naturally occurring Salmonella concentrations in non-inoculated feces ranged from 0.63 to 0.87 log₁₀ MPN/g in feces treated varying concentrations of Megasphaera elsdenii, and all Salmonella concentrations were statistically the same (p > 0.05).

The impact of treatment (p = 0.0720) and the treatment × time interaction (p = 0.4641) were not apparent for ruminal fluid samples not inoculated with Salmonella, but time of incubation did affect Salmonella recoveries (p = 0.0001). Naturally occurring Salmonella declined in non-inoculated ruminal fluid from 2.52 log MPN/g at 0 h to 1.91 log MPN/g at 72 h (Figure 1A; p < 0.0001).

The main effects of time, treatment, and the treatment × time interaction significantly (p < 0.0001) impacted antibiotic-susceptible Salmonella concentrations in feces treated with varying concentrations of Megasphaera elsdenii. Because the treatment × time interaction was significant, antibiotic-susceptible Salmonella data from feces are displayed and discussed according to sampling point (time) and Megasphaera elsdenii concentration (treatment). The largest antibiotic-susceptible Salmonella reduction (1.92 log MPN/g) was achieved between 0 and 72 h by the 2.5 × 10⁵ CFU/g M. elsdenii concentration (

Table 3. Mean concentration (log₁₀ MPN/g) of susceptible Salmonella concentration in inoculated cattle feces at 0, 24, 48, and 72 h following treatment with varying concentrations of Megasphaera elsdenii as an in vitro model.

Time Point (Hours)	Megasphaera elsdenii Target Concentration (CFU/g)
	0.0		1.0 × 105		2.5 × 105		5.0 × 105		5.0 × 108
	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM
0	4.36 A,a	0.06504	4.31 A,a	0.06504	4.44 A,a	0.06504	4.32 A,a	0.06504	4.31 A,a	0.06504
24	3.62 B,a,b	0.02313	3.54 B,b	0.02313	3.67 B,a	0.02313	3.64 B,a	0.02313	4.05 B,c	0.02313
48	3.54 B,a	0.03557	3.37 C,b	0.03557	2.54 C,c	0.03557	3.31 C,b,d	0.03557	3.18 C,d	0.03557
72	3.31 B,a	0.1186	2.44 D,b	0.1186	2.52 C,b	0.1186	2.68 D,b	0.1186	2.87 C,a,b	0.1186

Uppercase superscripts that vary within a column are statistically different (p ≤ 0.05) and are comparing one treatment across each sampling point. Lowercase superscripts that vary within a row are statistically different (p ≤ 0.05) and are comparing each treatment across a single sampling point. SEM indicates standard error of the mean.

; p < 0.0001). Antibiotic-susceptible Salmonella in the control feces (0.0 CFU/g of M. elsdenii) declined by 1.05 log MPN/g between the 0 and 72 h timepoints (p < 0.0001). At the 72 h timepoint, the largest population of antibiotic-susceptible Salmonella was recovered from control feces that were not treated with M. elsdenii (0.0 CFU/g of M. elsdenii), with 3.31 log MPN/g recovered in comparison to the 2.44 to 2.87 log MPN/g of Salmonella recovered from feces inoculated with varying concentrations of M. elsdenii.

Neither treatment (p = 0.7840) nor treatment × time interaction (p = 0.3746) impacted Salmonella counts for ruminal fluid samples inoculated with antibiotic-susceptible Salmonella, thus data are discussed only in accordance with the effect of time (p < 0.0001). Antibiotic-susceptible Salmonella populations in ruminal fluid declined from 3.41 log MPN/g at 0 h to 2.30 log MPN/g at 72 h (Figure 1B; p < 0.0001).

When sampling feces at 0, 24, 48, and 72 h following treatment with varying concentrations of Megasphaera elsdenii, the main effect of time (p < 0.001) and the treatment × time interaction (p = 0.0136) impacted Salmonella counts for feces inoculated with antibiotic-resistant Salmonella. Effects of Megasphaera elsdenii treatment were not evident (p = 0.4974). Because the treatment × time interaction was significant, antibiotic-resistant Salmonella data from feces are displayed and discussed according to the sampling point (time) and Megasphaera elsdenii concentration (treatment). The largest antibiotic-resistant Salmonella reduction (1.60 log MPN/g) was achieved between 0 and 72 h by the 2.5 × 10⁵ CFU/g M. elsdenii concentration (

Table 4. Mean concentration (log₁₀ MPN/g) of Salmonella that is resistant to one or more antibiotics in inoculated cattle feces at 0, 24, 48, and 72 h following treatment with varying concentrations of Megasphaera elsdenii as an in vitro model.

Time Point (Hours)	Megasphaera elsdenii Target Concentration (CFU/g)
	0.0		1.0 × 105		2.5 × 105		5.0 × 105		5.0 × 108
	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM	Log MPN/g	SEM
0	3.97 A,a	0.6618	4.00 A,B,a	0.6618	4.10 A,a	0.6618	3.93 A,B,a	0.6618	3.57 A,a	0.6618
24	3.67 A,a	0.3022	3.70 A,a	0.3022	3.27 A,a	0.3022	3.23 A,B,a	0.3022	3.80 A,a	0.3022
48	3.53 A,a	0.04092	3.40 A,a,b	0.04092	2.50 A,d	0.04092	3.30 A,b,c	0.04092	3.20 A,c	0.04092
72	3.30 A,a	0.1287	2.43 B,b	0.1287	2.50 A,b	0.1287	2.67 B,b	0.1287	2.90 A,a,b	0.1287

Uppercase superscripts that vary within a column are statistically different (p ≤ 0.05) and are comparing one treatment across each sampling point. Lowercase superscripts that vary within a row are statistically different (p ≤ 0.05) and are comparing each treatment across a single sampling point. SEM indicates standard error of the mean.

; p = 0.1283). Antibiotic-resistant Salmonella in the control feces (0.0 CFU/g of M. elsdenii) declined by 0.70 log MPN/g between the 0 and 72 h timepoints and this reduction was not significant (p = 0.7570). At the 72 h timepoint, the largest population of antibiotic-resistant Salmonella was recovered from control feces (0.0 CFU/g of M. elsdenii), with 3.30 log MPN/g recovered in comparison to the 2.43 to 2.90 log MPN/g of antibiotic-resistant Salmonella recovered from feces inoculated with varying concentrations of M. elsdenii. A large standard error was observed for samples collected at the 0 h sampling point, which impacted statistical differences when 0 h means were compared to other sampling points (Table 4).

The impact of treatment (p = 0.3813) and the treatment × time interaction (p = 0.4574) were not evident for ruminal fluid samples inoculated with antibiotic-resistant Salmonella. Time (p < 0.0001) was a significant main effect and data are only discussed according to the main effect of time. Antibiotic-resistant Salmonella concentrations in ruminal fluid declined from 3.36 log MPN/g at 0 h to 2.29 log MPN/g at 72 h (Figure 1C; p < 0.0001).

3.2. VFA and pH Analyses

The main effects of time, treatment, and the time × treatment interaction were not significant (p > 0.05) for acetate, propionate, isobutyrate, butyrate, isovalerate, valerate, isocaproate, caproate, and heptanoate in ruminal fluid and feces. The main effect of treatment, and the time × treatment interaction, did not significantly (p > 0.05) impact the pH of ruminal fluid or feces. The main effect of time did impact pH for ruminal fluid (p < 0.0001) or feces (p < 0.0001), with pH declining throughout the study. Ruminal fluid pH declined from 6.4 at 0 h to 5.6 at 72 h (Figure 2A; p < 0.0001) and fecal pH declined from 6.7 at 0 h to 5.9 at 72 h (Figure 2B; p < 0.0001).

4. Discussion

Supplementing finishing beef cattle diets with M. elsdenii has been shown to promote ruminal health [13,22] and improve dry matter intake [22]. Thus, from the perspective of animal performance and health, a benefit exists to supplementing finishing diets with this probiotic microorganism. However, the impact of M. elsdenii on Salmonella carriage in cattle has not been investigated. Therefore, this study was completed to address knowledge gaps surrounding efficacy of M. elsdenii as a pre-harvest intervention to reduce the burden of Salmonella in cattle.

In general, Salmonella populations declined in feces that were naturally or artificially contaminated. The pH of feces significantly declined over time (p ≤ 0.05) from 6.7 at 0 h to 5.9 at 72 h, which may have contributed to the decline in Salmonella populations. The largest reduction in antibiotic resistant and susceptible Salmonella populations was observed between 0 and 72 h, with a 1.92 log MPN/g (2.5 × 10⁵ CFU/g of M. elsdenii) reduction in antibiotic-susceptible Salmonella populations in inoculated feces. This reduction was 0.87 log MPN/g greater than the 1.05 log MPN/g reduction observed in the control feces inoculated with antibiotic-susceptible Salmonella. Similarly, at the 72 h timepoint, feces treated with M. elsdenii harbored fewer (p ≤ 0.05) antibiotic susceptible and resistant Salmonella populations than control feces, although the largest difference was 0.87 log MPN/g for both antibiotic susceptible and resistant Salmonella populations. Because these reductions are less than 1 log MPN/g, the efficacy of M. elsdenii at reducing antibiotic susceptible or resistant Salmonella in cattle feces should be considered marginal, as the biological relevance of reductions less than 1 log MPN/g is minimal, and additional research is necessary before efficacy can be determined.

The addition of M. elsdenii to feces did not significantly change VFA concentrations or pH (p > 0.05), although the pH of feces declined throughout the study (p ≤ 0.05). An increase in VFAs in feces has been associated with decreased populations of E. coli O157:H7 in the hindgut of cattle [15,16]. In the present study, M. elsdenii did not significantly alter VFA production, yet Salmonella populations generally declined throughout the study, with the largest reduction observed in feces treated with 2.5 × 10⁵ CFU/g of M. elsdenii. This suggests that 1) reductions were not associated with VFA concentration, or 2) given that only a 0.87 log MPN/g disparity was observed in fecal Salmonella populations at 72 h, the concentration of VFAs was consistently high enough in all samples to decrease Salmonella to a similar degree (within 1 log MPN/g difference). It is also important to note that pH and VFAs were determined from separate, non-inoculated fecal samples and may not fully represent the pH or VFA concentration of each inoculated sample.

The lack of a treatment effect suggests that M. elsdenii is not effective at reducing antibiotic susceptible or resistant Salmonella populations in cattle ruminal fluid when used as an intervention in an in vitro model. Although naturally occurring and inoculated Salmonella populations declined throughout the 72 h sampling period (Figure 1), these reductions were not associated with a treatment effect. The pH of ruminal fluid significantly declined over time (p ≤ 0.05) from 6.4 at 0 h to 5.6 at 72 h, which may have contributed to Salmonella population declines. Bolton et al. [23] also inoculated ruminal fluid with Salmonella and reported that changes in ruminal fluid pH (6.61 to 5.77) did not impact Salmonella populations, which suggests that pH changes in the present study may not have been responsible for reductions in Salmonella. It is also important to consider that cattle ruminal fluid consists of extensive native microbiota [17,24], which also provides competition for Salmonella and may impact survival. As mentioned previously, pH and VFAs were determined from separate, non-inoculated ruminal fluid samples and may not fully represent the pH or VFA concentration of each inoculated sample.

Megasphaera elsdenii is an important microorganism in the rumen of cattle [12,13] and is associated with VFA production [14]. However, the addition of M. elsdenii to ruminal fluid in the present study did not significantly change VFA concentrations or pH (p > 0.05). Bolton et al. [23] also discussed how the ruminal environment is relatively unfavorable for Salmonella due to VFAs; however, similar to the present study, also reported a reduction in Salmonella populations in the rumen that were not associated with VFA production.

5. Conclusions

The data presented herein provide preliminary evidence that M. elsdenii is not effective at reducing Salmonella in ruminal fluid but may be effective at marginally reducing Salmonella in cattle feces (<1 log MPN/g in comparison to control feces) when used in an in vitro model. The in vitro model presents challenges, however, including exposure to oxygen during sampling points, the lack of nutrient infusion (i.e., a bovine eating), and the accumulation of metabolic end-products during the 72 h study period. M. elsdenii is an anaerobic microorganism [14] and the viability may have declined due to exposure to oxygen during sample preparation and sampling periods when samples were not held under anaerobic conditions. The populations of M. elsdenii were not enumerated throughout the study due to challenges with selectivity and interference from the native microflora in ruminal fluid and feces. However, a method that can demonstrate M. elsdenii viability from even these complex matrices and a challenge model that does not require exposure to oxygen should be considered for future research. Ultimately, additional research is necessary, including in vivo feeding trials, before the efficacy of M. elsdenii at reducing the burden of Salmonella in cattle can be determined.